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European Journal of Pharmacology
|
September 22, 1992
The 5-HT2 receptor antagonist, MDL 28,133A, disrupts the serotonergic-dopaminergic interaction mediating the neurochemical effects of 3,4-methylenedioxymethamphetamine
C J Schmidt, C K Black, V L Taylor, et al.
Psychopharmacology
|
January 1, 1993
Electrophysiological, biochemical and behavioral evidence for 5-HT2 and 5-HT3 mediated control of dopaminergic function
M G Palfreyman, C J Schmidt, S M Sorensen, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 1, 1993
Characterization of the 5-HT2 receptor antagonist MDL 100907 as a putative atypical antipsychotic: behavioral, electrophysiological and neurochemical studies
S M Sorensen, J H Kehne, G M Fadayel, et al.
Molecular Pharmacology
|
October 1, 1990
Activity of 5,7-dichlorokynurenic acid, a potent antagonist at the N-methyl-D-aspartate receptor-associated glycine binding site
B M Baron, B L Harrison, F P Miller, et al.
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of 3
Search research articles
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Showing results (21-30 of 24) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 24 results.
European Journal of Pharmacology
|
September 22, 1992
The 5-HT2 receptor antagonist, MDL 28,133A, disrupts the serotonergic-dopaminergic interaction mediating the neurochemical effects of 3,4-methylenedioxymethamphetamine
C J Schmidt, C K Black, V L Taylor, et al.
Psychopharmacology
|
January 1, 1993
Electrophysiological, biochemical and behavioral evidence for 5-HT2 and 5-HT3 mediated control of dopaminergic function
M G Palfreyman, C J Schmidt, S M Sorensen, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 1, 1993
Characterization of the 5-HT2 receptor antagonist MDL 100907 as a putative atypical antipsychotic: behavioral, electrophysiological and neurochemical studies
S M Sorensen, J H Kehne, G M Fadayel, et al.
Molecular Pharmacology
|
October 1, 1990
Activity of 5,7-dichlorokynurenic acid, a potent antagonist at the N-methyl-D-aspartate receptor-associated glycine binding site
B M Baron, B L Harrison, F P Miller, et al.
Page
of 3